@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_head { this: np:hasAssertion dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_assertion; np:hasProvenance dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_provenance; np:hasPublicationInfo dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_publicationInfo; a np:Nanopublication . dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_assertion a np:Assertion . dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_provenance a np:Provenance . dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_publicationInfo a np:PublicationInfo . } dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_assertion { miriam-gene:5660 a ncit:C16612 . lld:C0017205 a ncit:C7057 . dgn-gda:DGNec0c5062e4953480ec286ee9738c2ba6 sio:SIO_000628 miriam-gene:5660, lld:C0017205; a sio:SIO_001121 . } dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_provenance { dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_assertion dcterms:description "[It was found that: (i) in the four Sap C-deficient cells PSAP was normally processed and sorted, the lack of Sap C being mainly due to the Sap C instability in late endosomal/lysosomal environment; (ii) the decrease/absence of Sap C affected the GCase intracellular localization; (iii) the lowest level of Sap C and enhanced autophagy were observed in the cells, which carried a Sap C mutation involving a cysteine residue; (iv) the four Sap C-deficient fibroblasts stored GC, ceramide and cholesterol, the last two lipids being clearly localized in lysosomes; (v) a correlation was observed between the type of Sap C mutation and the Gaucher phenotype: apparently, mutations involving cysteine residues lead to a neurological variant of GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:20484222; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP707550.RAb-67IxQ6PpW0qdhPsaBh44QdFf2kibAhQZxgswrnLnk130_publicationInfo { this: dcterms:created "2014-10-02T12:39:10+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }